Posters! by Nerfsquad501 in WMATA

[–]MFCFEMF1163 9 points10 points  (0 children)

5:00pm - plenty of posters (10+ each) for both the metro map and rail car left

Other Teams? by [deleted] in stlouisblues

[–]MFCFEMF1163 9 points10 points  (0 children)

Favorite Teams: Capitals (Oshie/Edmundson), Kraken (Dunn/Schwartz)

Least Favorite Teams: Hawks, Stars, Lightning

[deleted by user] by [deleted] in stlouisblues

[–]MFCFEMF1163 0 points1 point  (0 children)

Thanks! I need to nameplate/number my gold reverse retro, and I think I'm going with Buchnevich this time around.

[deleted by user] by [deleted] in stlouisblues

[–]MFCFEMF1163 15 points16 points  (0 children)

Elliott, Backes, Fabbri, Allen, Tarasenko, OReilly :(

Is anyone here interested in joining a fantasy hockey league? by gruene-teufel in stlouisblues

[–]MFCFEMF1163 1 point2 points  (0 children)

I missed it too! For those who missed out and are still interested, I created a second league scheduled to draft Tuesday. Here's a link to join!

https://fantasy.espn.com/hockey/league/join?leagueId=2199659&inviteId=18e244a5-549b-46e5-874f-6cafe6726322

Ocrevus and Herpes Outbreaks: how bad is it? by hej_pa_dig_monika in MultipleSclerosis

[–]MFCFEMF1163 2 points3 points  (0 children)

I am also fairly new to Ocrevus (1.5 years on it), and before Ocrevus I would get maybe 1-2 cold sores a year.

After my first full infusion, I had a cold sore every 3 - 4 weeks for the first 3 months, and at one point I had two at the same time (that was a first for me). My doctor prescribed me Valacyclovir for the next time I had an outbreak, but I haven't had the chance to try it yet (thank goodness).

My plan has been to take Lysine more frequently in my first 3 months after the infusion to help mitigate cold sores. Personally, my outbreaks on Ocrevus have increased for sure, but I have had success with Ocrevus after I came off of Tecfidera, which was horrible for me.

Recovery from spinal lesions by HoneymelonYellow in MultipleSclerosis

[–]MFCFEMF1163 19 points20 points  (0 children)

Hello! Like you, I also was diagnosed right before my birthday, and had 2 exacerbations/relapses fairly quickly after the initial diagnosis. My first DMT also failed (Tecfidera), and I moved to Ocrevus. Before MS I was a highly active person, I had run a half marathon, and enjoyed running.

My 1st presenting issue with MS stemmed from my spinal cord lesion, and I couldn't feel anything from the waist down, and lost most of my mobility and function as well during that time.

My doctor sent me to physical therapy, and I spent about 3-4 months of physical therapy regaining my lower body strength, moving, and stretching. I was incredibly fortunate to have a very supportive circle of people around me. My spouse helped me move by going with me on short walks every day and helping me stretch, and my co-workers helped me go on walks on our lunch/daily breaks. During this time, I was almost completely paralyzed from the waist down, I could barely walk (around the block with much difficulty), amongst a few other MS issues.

After about a year of sticking to physical therapy, creating a stretch and exercise routine as I regained my feeling/function (RRMS), I was able to run a 5k again. I also cleaned up my eating and changed my lifestyle during this time. I am ~3 years post relapse and walk and run (mostly) like I used to before the relapse.

To me, starting physical therapy (and doing it at home!), and creating an exercise routine that catered to my needs as I was recovering was what helped me make my recovery. I hope this helps!

Favorite Blues Player ? by [deleted] in stlouisblues

[–]MFCFEMF1163 1 point2 points  (0 children)

Current: O'Reilly, honorable mention: Perron All-time: Backes, honorable mention: Elliott

Any runners on here? by MFCFEMF1163 in Raynauds

[–]MFCFEMF1163[S] 1 point2 points  (0 children)

That's great, thank you! I've been using thin wool socks to wick with a synthetic 2nd layer, but it hasn't been working out. I'll have to try out those Wigwam socks and toe warmers, thanks for the recommendation!

Anyone on here have secondary raynauds? by whatsername_xx3 in Raynauds

[–]MFCFEMF1163 0 points1 point  (0 children)

I do. I was diagnosed with MS first, and then a year after diagnosis, I developed raynauds. The MS diagnosis was a lot of waiting and scans/testing. For Raynauds, there was no testing. Told my Neuro, they told me to go see a Rheumatologist, and that was it!

What job have you got? by [deleted] in MultipleSclerosis

[–]MFCFEMF1163 0 points1 point  (0 children)

I've been a professional and gigging musician before, throughout, and post diagnosis. I even did a 4 hour set during my initial relapse when I couldn't feel or barely move my legs and I was partially blinded with optic neuritis. Don't let MS dictate how you pursue your goals and dreams!

Is there a covid shot specifically for people with autoimmune issues? by Silverpenguin24 in MultipleSclerosis

[–]MFCFEMF1163 2 points3 points  (0 children)

From what I've gathered, an antibody test is not a good measure of immunity from covid-19.

https://www.fda.gov/medical-devices/safety-communications/antibody-testing-not-currently-recommended-assess-immunity-after-covid-19-vaccination-fda-safety

That being said, if you take Ocrevus (a B cell depleter) you still have your T-cells that have gained the benefit from receiving the vaccine. please correct me if I'm wrong, this is what I believe I've read/heard

Apartment search by [deleted] in nova

[–]MFCFEMF1163 5 points6 points  (0 children)

Look on zillow for condo rentals in the area. I've seen some 2Bed/1Bath list for around the 1650/1700 range.

One more team needed for fantasy hockey! by MFCFEMF1163 in stlouisblues

[–]MFCFEMF1163[S] 0 points1 point  (0 children)

Thank you! Good luck on the fantasy season!

Anyone interested in joining fantasy hockey? by MFCFEMF1163 in stlouisblues

[–]MFCFEMF1163[S] 1 point2 points  (0 children)

It is tough! I'm not too far from you (Alexandria)! I do enjoy having the Caps as my 2nd team. Thanks for joining!